Activity, participation, and quality of life 6 months poststroke
- Författare
- Mayo NE, Wood-Dauphinee S, Cote R, Durcan L, Carlton J.
- Titel
- Activity, participation, and quality of life 6 months poststroke
- Utgivningsår
- 2002
- Tidskrift
- Archives of Physical Medicine and Rehabilitation
- Volym
- 83
- Häfte
- 8
- Sidor
- 1035-42
- Sammanfattning
Mayo NE, Wood-Dauphinee S, Côté R, Durcan L, Carlton J. Activity, participation, and quality of life 6 months poststroke. Arch Phys Med Rehabil 2002;83:1035-42. Objectives: To estimate the extent of activity and participation of individuals 6 months poststroke and their influence on health-related quality of life (QOL) and overall QOL, information that would be useful in identifying services that stroke patients would need in the community. Design: Inception cohort study. Setting: Ten acute care hospitals in metropolitan areas of the province of Quebec. Participants: Persons with first-ever stroke, either ischemic or hemorrhagic. In parallel, a population-based sample of community-dwelling individuals without stroke, frequency matched in age and city district, were also recruited. Interventions: Not applicable. Main Outcome Measures: Stroke subjects were interviewed by telephone at 6-month intervals for 2 years of follow-up. The community-dwelling individuals without stroke were also followed. Results: A total of 434 persons were interviewed approximately 6 months poststroke. Their average age ± standard deviation was 68.4±12.5 years; the average age of the 486 controls was 61.7±12.4 years. The stroke group scored on average 90.6/100 on the Barthel Index; 39% reported a limitation in functional activities, 54% reported limitations with higher-level activities of daily living such as housework and shopping, and 65% reported restrictions in reintegration into community activities. By using the Medical Outcomes 36-Item Short-Form Health Survey (SF-36), persons with stroke rated their physical health 7 points lower than healthy peers; also, 7 of the 8 subscales of the SF-36 were affected by stroke. Conclusion: Almost 50% of the community-dwelling stroke population lived with sequelae of stroke such that, unless there was a full-time and able-bodied caregiver at home, they needed some form of home help. A large proportion also reported lack of meaningful activity, indicating a need for organized support groups for people with stroke; otherwise, boredom will lead to depression and worsening of function, affect, health status, and QOL. © 2002 by the American Congress of Rehabilitation Medicine and the American Academy of Physical Medicine and Rehabilitation